Creavo Vitalscan Magnetocardiograph
K-Number: K170154 · 2017-10-12
ApplicantCreavo Medical Technologies, Ltd.
Decision Date2017-10-12
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Creavo Vitalscan Magnetocardiograph is a medical device manufactured by Creavo Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2017-10-12 under approval number K170154. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Creavo Vitalscan Magnetocardiograph?
Creavo Vitalscan Magnetocardiograph is a medical device that received FDA 510(k) clearance on 2017-10-12. It is manufactured by Creavo Medical Technologies, Ltd.. The 510(k) number is K170154.
When was Creavo Vitalscan Magnetocardiograph approved by the FDA?
Creavo Vitalscan Magnetocardiograph received FDA 510(k) clearance on 2017-10-12, under approval number K170154.
What company makes Creavo Vitalscan Magnetocardiograph?
Creavo Vitalscan Magnetocardiograph is manufactured by Creavo Medical Technologies, Ltd..
What is the FDA product code for Creavo Vitalscan Magnetocardiograph?
The FDA product code for Creavo Vitalscan Magnetocardiograph is DPS.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.